rs730882203, DMBX1

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hearing Loss
CUI: C3887873
Disease: Hearing Loss
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.700 GeneticVariation CLINVAR
Hyperopia
CUI: C0020490
Disease: Hyperopia
0.700 GeneticVariation CLINVAR
Strabismus
CUI: C0038379
Disease: Strabismus
0.700 GeneticVariation CLINVAR